1268492-92-7 Usage
Uses
Used in Organic Synthesis:
[(3S)-3-fluorooxolan-3-yl]Methanol is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique reactivity and stereochemistry make it a valuable component in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
[(3S)-3-fluorooxolan-3-yl]Methanol is used as an intermediate in the development of pharmaceutical compounds. The presence of the fluorine atom and the specific stereochemistry may provide advantages in the design and synthesis of new drugs with improved properties.
Used in Agrochemical Industry:
[(3S)-3-fluorooxolan-3-yl]Methanol is used as a starting material or intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique properties may contribute to the development of more effective and environmentally friendly products.
Further research and evaluation of [(3S)-3-fluorooxolan-3-yl]Methanol's properties and potential uses may be warranted to fully understand its applications and benefits in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1268492-92-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,4,9 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1268492-92:
(9*1)+(8*2)+(7*6)+(6*8)+(5*4)+(4*9)+(3*2)+(2*9)+(1*2)=197
197 % 10 = 7
So 1268492-92-7 is a valid CAS Registry Number.
1268492-92-7Relevant articles and documents
A broadly applicable and practical oligomeric (salen)Co catalyst for enantioselective epoxide ring-opening reactions
White, David E.,Tadross, Pamela M.,Lu, Zhe,Jacobsen, Eric N.
, p. 4165 - 4180 (2014/06/09)
The (salen)Co catalyst (4a) can be prepared as a mixture of cyclic oligomers in a short, chromatography-free synthesis from inexpensive, commercially available precursors. This catalyst displays remarkable enhancements in reactivity and enantioselectivity relative to monomeric and other multimeric (salen)Co catalysts in a wide variety of enantioselective epoxide ring-opening reactions. The application of catalyst 4a is illustrated in the kinetic resolution of terminal epoxides by nucleophilic ring-opening with water, phenols, and primary alcohols; the desymmetrization of meso epoxides by addition of water and carbamates; and the desymmetrization of oxetanes by intramolecular ring opening with alcohols and phenols. The favorable solubility properties of complex 4a under the catalytic conditions facilitated mechanistic studies, allowing elucidation of the basis for the beneficial effect of oligomerization. Finally, a catalyst selection guide is provided to delineate the specific advantages of oligomeric catalyst 4a relative to (salen)Co monomer 1 for each reaction class.
